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Maxima Radiopaque Ant

HENRY SCHEIN, INC. · Model 2286569 · UDI-DI 00304040000847

ELM Prescription
10
510(k) clearances
56
Adverse events
0
Recalls
103
Facilities

Description

Maxima Radiopaque Ant

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.